Table 2. Demographics, Microbiology, and Clinical Outcomes of Patients With Invasive Meningococcal Disease Included in the Analysis in a Study of the Association of a Meningococcus Group B Vaccine With Group B Invasive Meningococcal Disease Among Children in Portugal.
Characteristic | No. (%) | ||||
---|---|---|---|---|---|
Cases with group B disease aged ≥134 d (primary analysis; n = 69)a | Cases with any invasive meningococcal disease aged ≥134 d (n = 85)a | Cases with group B disease aged ≥74 d (n = 82)a | Cases with any invasive meningococcal disease aged ≥74 d (n = 98)a | ||
Age, median (IQR), mo | 24.1 (10.1-50.1) | 24.1 (9.6-51.3) | 17.5 (6.2-43.6) | 17.5 (7.1-48.5) | |
Sex | |||||
Male | 42 (60.9) | 54 (63.5) | 49 (59.8) | 61 (62.2) | |
Female | 27 (39.1) | 31 (36.5) | 33 (40.2) | 37 (37.8) | |
Diagnosisb | |||||
Septicemia and meningitis | 32 (46.4) | 33 (38.8) | 38 (46.3) | 39 (39.8) | |
Meningitis | 16 (23.2) | 23 (27.1) | 20 (24.4) | 27 (27.6) | |
Septicemia | 14 (20.3) | 19 (22.4) | 16 (19.5) | 21 (21.4) | |
Bacteremia | 6 (8.7) | 8 (9.4) | 7 (8.5) | 9 (9.2) | |
Arthritis | 1 (1.4) | 2 (2.4) | 1 (1.2) | 2 (2.0) | |
Duration of admission, median (IQR), d | 8 (7-10) | 7 (6-10) | 8 (7-10) | 7 (7-10) | |
Outcomec | |||||
Alive with no sequelae | 49 (71.0) | 64 (75.3) | 60 (73.2) | 75 (76.5) | |
Alive with sequelae | 15 (21.7) | 15 (17.6) | 16 (19.5) | 16 (16.3) | |
Developmental delay | 9 (13.0) | 9 (10.6) | 10 (12.2) | 10 (10.2) | |
Death | 5 (7.2) | 6 (7.1) | 6 (7.3) | 7 (7.1) | |
Amputation | 4 (5.8) | 4 (4.7) | 4 (4.9) | 4 (4.1) | |
Deafness | 1 (1.4) | 1 (1.2) | 1 (1.2) | 1 (1.0) | |
Other | 1 (1.4) | 1 (1.2) | 1 (1.2) | 1 (1.0) | |
Meningococcal capsular groupd | |||||
B | 69 (100) | 69 (81.2) | 82 (100) | 82 (83.7) | |
Y | 0 | 11 (12.9) | 0 | 11 (11.2) | |
W | 0 | 4 (4.7) | 0 | 4 (4.1) | |
Z | 0 | 1 (1.2) | 0 | 1 (1) |
Abbreviation: IQR, interquartile range.
The youngest valid age for partial vaccination was 74 days and for full vaccination was 134 days.
Diagnoses at hospital discharge were options provided on the case report forms to reporting clinicians without strict definition. Twelve children and adolescents were transferred from secondary to tertiary care facilities.
Outcomes were extracted from the medical records accessed at the time of data collection, so they reflect information obtained both during admission and follow-up.
Meningococcal capsular grouping was done by polymerase chain reaction, as recommended by the World Health Organization.14